ProfileGDS1065 / 213186_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 74% 77% 75% 74% 79% 77% 74% 74% 74% 75% 78% 78% 76% 78% 76% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1131.874
GSM24653Normal subject 2142.377
GSM24654Normal subject 3169.475
GSM24655A3243G-MELAS subject 18374
GSM24656A3243G-MELAS subject 2172.379
GSM24657A3243G-MELAS subject 3232.377
GSM24658A3243G-MELAS subject 4119.774
GSM24659A3243G-PEO subject 196.674
GSM24660A3243G-PEO subject 2111.774
GSM24661A3243G-PEO subject 394.175
GSM24662A3243G-PEO subject 4127.378
GSM24663mtDNA "Common"-deletion subject 1171.878
GSM24664mtDNA "Common"-deletion subject 2252.676
GSM24665mtDNA "Common"-deletion subject 3242.878
GSM24666mtDNA "Common"-deletion subject 4249.776